State
73,566 recalls have nationwide distribution and so reach New York. 12,947 additional recalls listed New York specifically in their distribution scope.
Of the 12,947 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,698 (29%) are Severe.
Which agencies issued them
These figures cover only the 12,947 recalls whose distribution notice names New York specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fruit Fresh Up, Inc. is recalling Eden Valley Bulk Fruit Salad which may be contaminated with Listeria monocytogenes. The recall affects 39,232 units distributed in New York, Massachusetts, and Pennsylvania.
NTN Bearing Corporation is recalling specific driveshafts because internal components may not have been heat-treated properly. This defect could lead to driveshaft failure and a sudden loss of drive power.
Adamis Pharmaceuticals is recalling SYMJEPI epinephrine injections due to potential needle clogging that may prevent medication delivery. The FDA has classified this as a Class I recall affecting nationwide distribution.
Fruit Fresh Up, Inc. is recalling Fresh Harvest Small veggie platters with ranch that may be contaminated with Listeria monocytogenes. Affected products were distributed in New York, Massachusetts, and Pennsylvania.
Tops Dill Dip Bulk is being recalled due to potential contamination with Listeria monocytogenes. Consumers should stop using the product and dispose of it safely.
Adamis Pharmaceuticals is recalling 2,500 cartons of SYMJEPI (epinephrine injection) nationwide due to a defective delivery system that may clog the needle and prevent medication dispensing.
Fruit Fresh Up, Inc. recalls MapleVale 18# Wet Salad Bucket due to potential Listeria monocytogenes contamination. Affected products were distributed in New York, Massachusetts, and Pennsylvania.
Lexus is recalling 2022 NX250, NX350, NX350h, and NX450h+ vehicles because missing spot-welds may cause the front shock absorber to separate, increasing crash risk.
Top Quality Produce Enoki Mushrooms are recalled due to Listeria monocytogenes contamination detected by California Department of Public Health. The recall affects 1108 cases distributed across six states.
Pfizer is recalling quinapril HCl/hydrochlorothiazide tablets due to manufacturing defects that allowed N-nitroso impurities to exceed acceptable daily intake limits. Patients taking affected lots should contact their pharmacy.
Bread Alone, Inc. is recalling Fruit & Nut Sourdough bread because it contains undeclared sulfites. The affected product includes all loaves with expiration dates through March 28, 2022, distributed in New York, Massachusetts, and Connecticut.
Stradis Medical is recalling Anterior Hip Pack surgical kits due to perforated or torn outer bags that may compromise sterility. No illnesses have been reported.
BMW is recalling 2022-2023 iX vehicles due to incorrect software in the air bag control unit. The malfunction indicator light may not illuminate if the air bag system has a problem, increasing crash injury risk.
Certain Toyota and Lexus vehicles may have a software defect preventing the Electronic Stability Control system from re-engaging after being manually disabled. Dealers will update the software free of charge.
Pfizer is recalling 53 bottles of Accuretic blood pressure tablets nationwide due to manufacturing impurities that exceed FDA acceptable daily intake limits. The affected lot is FG5379, expiring August 2024.
Nissan is recalling 2020 Sentra vehicles with LED headlights because the right-hand headlight may be misaligned, potentially reducing visibility and increasing crash risk.
Merck is recalling 3,600 cartons of Janumet (sitagliptin/metformin HCl) tablets nationwide due to the presence of stainless steel particulates in the tablets.
Keystone RV is recalling 2022 Crossroads Zinger travel trailers because the furnace vent extension may not have been installed. A missing vent can allow carbon monoxide to enter the living area.
Philips is recalling adult Smart PADS cartridges for HeartStart HS1 defibrillators due to potential gel separation from the pad backing. Affected pads may have reduced gel contact, potentially affecting device performance.
Abbott Molecular recalled Alinity m HBV Application Specification Files due to potential for incorrect high quantitation results on negative samples, which could affect test accuracy for hepatitis B virus detection.
Pfizer is recalling Accuretic (quinapril/hydrochlorothiazide) tablets nationwide due to N-nitroso impurities exceeding acceptable daily intake limits. The impurity resulted from a manufacturing deviation.
Pfizer is recalling Accuretic blood pressure tablets due to manufacturing deviations that resulted in N-nitroso chemical impurities exceeding safe intake limits. Patients should contact their pharmacist or physician.
SyncVision cardiac imaging systems may display incorrect measurements during same-session procedures if workflow steps are performed out of order, potentially affecting patient treatment.
Vitae Enim Vitae Scientific, Inc. is recalling Phenobarbital Sodium Injection nationwide due to deviations from Current Good Manufacturing Practices (CGMP) that raise concerns about product sterility.
Abbott Molecular is recalling the Alinity m HBV AMP Kit due to potential for falsely high results on negative samples. The kits are used for Hepatitis B virus testing in the US and internationally.